Actively Recruiting
MENTOR Wellness Program
Led by NYU Langone Health · Updated on 2026-01-28
138
Participants Needed
1
Research Sites
172 weeks
Total Duration
On this page
Sponsors
N
NYU Langone Health
Lead Sponsor
N
National Institute on Disability, Independent Living, and Rehabilitation Research
Collaborating Sponsor
AI-Summary
What this Trial Is About
This randomized trial aims to determine the effectiveness a virtual wellness intervention program in individuals with traumatic brain injury (TBI). Participants will be randomized at enrollment into two groups: immediate treatment (IT) and delayed treatment (DT) group. This study will also provide insights into the impact of these intervention's components in helping emotional, physical, and nutritional outcomes post-injury in the context of social determinants of health (SDOH).
CONDITIONS
Official Title
MENTOR Wellness Program
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Have a medically-documented complicated-mild, moderate, or severe traumatic brain injury requiring admission to an acute inpatient rehabilitation unit
- Be at least 12 months post-traumatic brain injury
- Have access to the internet on a computer, tablet, and/or smartphone
- Speak and understand English or Spanish
- Agree to participate
- Medically cleared by a recognized health professional (primary physician, physiatrist, neurologist, rehabilitation therapist, or other) to participate in the study
You will not qualify if you...
- No history of complicated-mild, moderate, or severe traumatic brain injury
- Less than 12 months post-traumatic brain injury
- In minimally conscious or vegetative state
- Beginning a new treatment regimen at study start that could influence study findings (physical therapy, occupational therapy, vestibular therapy, psychotherapy, medication), unless treatment is stable
- Significant cognitive impairment (delirium or dementia) preventing meaningful consent or data collection
- Significant or major disabling medical condition preventing meaningful consent or data collection
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
NYU Langone Health
New York, New York, United States, 10016
Actively Recruiting
Research Team
F
Fatima Imdad
CONTACT
M
Michelle Michelle.Smith@nyulangone.org
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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